Literature DB >> 1728542

Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.

S Cutillo1, L Pinto, B Nobili, E Miraglia del Giudice, A Iolascon.   

Abstract

Recently it has been clearly established that partial deficiency of spectrin (SP) evaluated by radioimmunoassay is a common feature of many different forms of hereditary spherocytosis (HS). In this paper the determination of SP density (spectrin/band 3 ratio) in 46 HS patients and in 50 normal controls is presented. The comparison between the membrane SP density of HS subjects and controls showed a statistically significant difference (P less than 0.0005). Moreover no overlap between normal and HS subjects was observed. Membrane spectrin/band 3 ratio has been found related to some clinical features: indeed patients with severe HS showed a smaller SP density than those with milder HS. Our results show that the evaluation of membrane SP density permits a prompt diagnosis of HS and avoids extensive and unnecessary studies for other anaemias.

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Year:  1992        PMID: 1728542     DOI: 10.1007/bf02073887

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  14 in total

Review 1.  HEREDITARY SPHEROCYTOSIS: A DISEASE OF THE RED CELL MEMBRANE.

Authors:  H S JACOB
Journal:  Semin Hematol       Date:  1965-04       Impact factor: 3.851

2.  The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes.

Authors:  J T DODGE; C MITCHELL; D J HANAHAN
Journal:  Arch Biochem Biophys       Date:  1963-01       Impact factor: 4.013

3.  Genetics of spherocytosis.

Authors:  N E MORTON; A A MACKINNEY; N KOSOWER; R F SCHILLING; M P GRAY
Journal:  Am J Hum Genet       Date:  1962-06       Impact factor: 11.025

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  Occurrence of hereditary spherocytosis and beta thalassaemia in the same family: globin chain synthesis and visco diffractometric studies.

Authors:  B Pautard; C Feo; D Dhermy; H Wajcman; V Baudin-Chich; J Delobel
Journal:  Br J Haematol       Date:  1988-10       Impact factor: 6.998

6.  Deficient red-cell spectrin in severe, recessively inherited spherocytosis.

Authors:  P Agre; E P Orringer; V Bennett
Journal:  N Engl J Med       Date:  1982-05-13       Impact factor: 91.245

7.  High prevalence of increased osmotic fragility of red blood cells among Norwegian blood donors.

Authors:  H C Godal; H Heistø
Journal:  Scand J Haematol       Date:  1981-07

8.  Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.

Authors:  P Agre; A Asimos; J F Casella; C McMillan
Journal:  N Engl J Med       Date:  1986-12-18       Impact factor: 91.245

9.  Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.

Authors:  P Agre; J F Casella; W H Zinkham; C McMillan; V Bennett
Journal:  Nature       Date:  1985 Mar 28-Apr 3       Impact factor: 49.962

10.  Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.

Authors:  J A Chasis; P Agre; N Mohandas
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808

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